Calculation of retention factors in capillary electrochromatography from chromatographic and electrophoretic data

Retention factors in capillary electrochromatography (CEC) were calculated by means of theoretically derived equations and experimentally determined parameters in microcolumn liquid chromatography and capillary zone electrophoresis. It was found that the retention factor of uncharged components in CEC was about 20% higher than was calculated. The derived equations do not take into account alteration of the nature of the stationary phase or distribution constant by the applied electric field. However, the influence of the electric field on the retention in CEC can be estimated. Individual field contributions could not be determined.     

Gas chromatographic retention data of wax esters

Higher wax esters within the range of C24 to C44 (205 standards) were analyzed by means of gas chromatography and Kováts indexes (I) and reduced Kováts indexes (RKI) were calculated. The dependences of these retention data on number of carbon atoms and on number and position of double bonds in acid and in alcohol moieties of esters were plotted.     

Mosaic increments for predicting the gas chromatographic retention data of the chlorobenzenes

The chlorinated organic compounds are very important from the point of view of the chemical industry and environmental protection, and therefore the gas chromatographic analysis of these compounds is very interesting for analytical chemists. In this paper we studied the relationship between the molecular structure and gas chromatographic retention on several stationary phases having different polarity and at several temperatures of benzene and 12 chlorobenzene compounds as model compounds. A coding system involving primary (mosaic increments) and secondary (bond increments)calculation methods was developed. The retention indices of benzene and the chlorobenzenes calculated on HP-5 at 120 degrees C shows a better performance of the mosaic increments (average absolute deviation delta of 1.7 retention index units) compared with the bond increments (delta = 11.7 retention index units). Retention factors, k, calculated with mosaic increments for chlorobenzenes on SPB-1 and WAX-10, at 140 degrees C, yield average relative errors of epsilon = 0.9 and 3.5%, respectively. Therefore, the presented paper provides a new possibility for precalculation of the retention data.     

Determining the vapour pressures of plant volatiles from gas chromatographic retention data

The frequently used vapour pressure versus Kováts retention index relationship has been evaluated in terms of its universal applicability, highlighting the problems associated with predicting the vapour pressures of structurally divergent organic compounds from experimentally measured isothermal Kováts retention indices. Two models differing in approximations adopted to express the activity coefficient ratio have been evaluated using 32 plant volatiles of different structural types as a test set. The validity of these models was established by checking their ability to reproduce 22 vapour pressures known from independent measurements. Results of the comparison demonstrated that (i) the original model, based on the assumption of equal activity coefficients for the test and reference substances, led, as expected, to a poor correlation (r2 = 89.1% only), with significantly deviating polar compounds and (ii) the model showed significant improvement after incorporating a new empirical term related to vaporization entropy and boiling point. The addition of this term allowed more than 99% of the vapour pressure variance to be accounted for. The proposed model compares favourably with existing correlations, while having an added advantage of providing a convenient tool for vapour pressure determination of chemically divergent chemicals.     

Multivariate analysis of chromatographic retention data and lipophilicity of phenylacetamide derivatives

One of the most important physicochemical parameters of a molecule that determines its bioactivity is its lipophilicity. Cluster analysis (CA), principal component analysis (PCA), and sum of ranking differences (SRD) were used to compare the lipophilic parameters of twenty phenylacetamide derivatives, obtained experimentally as chromatographic retention data in the presence of different solvents and calculated by different mathematical methods. All the applied methods of multivariate analysis gave approximately similar grouping of the studied lipophilic parameters. In the attempt to group the investigated compounds in respect of their lipophilicity, the obtained results appeared to be dependent on the applied chemometric method. The CA and PCA, grouped the compounds on the basis of the nature of the substituents R₁ and R₂, indicating that they determine to a great extent the lipophilicity of the investigated molecules. Unlike them, the SRD method could not be used to group the studied compounds on the basis of their lipophilic character.     

Modeling of retention behavior in capillary electrochromatography from chromatographic and electrophoretic data

A phenomenological approach was presented to describe the retention behaviors of solutes in capillary electrochromatography (CEC). Equations for calculation of the retention time and actual chromatographic retention factor for ionic solutes, weak monoprotic acid and weak monoprotic base were derived, which can be described by two general expressions regardless the charge status of the solute. The general expressions enable calculation of the retention time and retention factor in CEC from chromatographic and electrophoretic data, which were experimentally verified with a variety of compounds and a variety of CEC modes. Based on this approach, the chromatographic retention and the electrophoretic migration in the CEC systems studied were found to be two independent processes. The validity of this approach was also discussed.     

A study of solid surface polarity using inverse gas chromatographic retention data

Summary Sensitivities of a solid surface to dispersive and nondispersive (polar) interactions can be readily estimated by a multiple regression analysis of inverse gas chromatographic retention data of a set of probe solutes. This analysis is based on linear free energy relationships (LFERs). The sensitivity to the latter type of interactions can be used as a measure of the surface polarity of the solid. This has been shown in the case of a graphitized carbon fiber and the method is also applicable to other solids.     

Repeatability and reproducibility of retention data and band profiles on six batches of monolithic columns

Chromatographic data were acquired for eight different mixtures, under five different sets of experimental conditions, for a total of 30 neutral, acidic and basic test compounds, on a series of six Chromolith Performance columns from Merck. These columns are made of a C₁₈ chemically bonded silica monolith. Each column belonged to a different production batch, so the data reported here characterize their batch-to-batch reproducibility. The parameters studied in this work were the retention times, the retention and separation factors, the hydrophobic and the steric selectivities, the column efficiencies, and the tailing factors for all 30 compounds.     

Ion chromatographic separation of car☐ylic acids prediction of retention data

The retention behavior of biologically relevant monovalent (formic, acetic, propionic, lactic and pyruvic) and divalent (oxalic, malonic, succinic, fumaric, maleic and tartaric acids) car☐ylic acids together with inorganic analytes (chloride and sulphate) has been studied. The separation was performed on a latex-based strong anion-exchange resin using carbonate buffer systems in suppressed IC. The retention behaviour of analytes was investigated at different pH values and [HCO₃⁻]+[CO₃²⁻] concentrations. A theoretical model, involving ion-exchange equilibria of sample and eluent anions, was derived and applied to the chromatographic data obtained. Chromatographic ion exchange selectivity values were determined and retention data were calculated for the anions using different carbonate eluent conditions. The average of errors between the predicted and the measured retention volumes of the analytes studied does not exceed 4.0%. The study effectively characteristics the behaviour of different analytes under elution conditions of practical importance.     

Interpreting the gas chromatographic retention of n-alkanes

Non-linear regressions were applied to n-alkanes retention data for the determination of gas hold-up in a preceding paper. It was found that at temperatures over 100 degrees C the reduced partial molar free energy of solution, deltaG/RT, tends to be negligible for the solute methane in poly(dimethylsiloxane) stationary phases. A consequence of interest can be inferred from this fact. The C-H bonds from terminal methyl groups of n-alkane solute molecules should not contribute significantly to deltaG/RT in these conditions. The analysis of data confirms that, within the chromatographic experimental error, the contributions of n-alkane end C-H bonds are also negligible in this temperature range. Consequently, the regression parameter that contains the phase ratio of the column only includes the gas hold-up as the accompanying factor.     

Correlation of supercritical-fluid extraction recoveries with supercritical-fluid chromatographic retention data: A fundamental study

The possibility of using supercritical-fluid chromatographic retention data for examining the effects of operational parameters, such as pressure and flow rate, on the extraction characteristics in supercritical-fluid extraction (SFE) was investigated. A model was derived for calculating the extraction efficiency in SFE from retention data and peak shapes measured in supercritical-fluid chromatography (SFC). By performing the SFC experiments at the same pressure and temperature as the SFE extractions using the SFE extraction cell as the SFC column, an accurate prediction of extraction efficiencies could be made. Finally, the effects of matrix composition and analyte concentration on extraction efficiency were studied.     

烯烃气相色谱保留指数的QSRR研究

通过对184个烯烃类化合物在不同固定相不同柱温下的617个样本的气相色谱保留指数值(RI)与其部分参数:拓扑指数(mQ)、偶极矩(DPL)、固定液极性值(CP)及柱温(T)建立定量-色谱保留相关(QSRR)模型.分别利用多元线性回归(MLR)、偏最小二乘回归(PLSR)、人工神经网络(ANN)建模,同时采用内部及外部双重验证的办法对所得模型稳定性能进行深入分析和检验,建模计算值、留一法(LOO)交互检验(CV)预测值和外部样本的复相关系数Rcum,QLOO和Rext分别为0.999 2,0.998 4和0.999 2(MLR);0.999 0,0.998 0和0.999 1(PLSR);0.999 4,0.998 7和0.999 2(ANN).结果表明:所建定量结构保留关系(QSRR)模型具有良好的稳定性和预测能力,较好地揭示了烯烃类化合物在不同固定相不同柱温上气相色谱保留指数的变化规律.     

三聚氰胺在双色谱柱串联模式下的色谱保留研究

研究了亲水相互作用色谱柱串联C_(18)柱上三聚氰胺的色谱保留,并应用牛奶基质中三聚氰胺的高效分离。将HILIC柱与C_(18)柱串联,研究不同色谱柱串联顺序及色谱分离条件下三聚氰胺的保留情况,结果表明:当流动相为乙腈-乙酸铵(10mmol/L)=85∶15(v/v)、柱温30℃、流速0.75mL/min、检测波长220nm、HILIC柱在前C_(18)柱在后串联时,三聚氰胺分离效果最佳。在最佳的色谱条件下,对市售牛奶进行测定,未检测出三聚氰胺,加标回收率在81.1%～119%,三聚氰胺在双柱模式下分析效果良好。     

The influence of various factors on the gas chromatographic separation of certain diastereoisomers

Conclusions Not the nature of the stationary phase, but the ratio of the vapor pressures of the diastereoisomers makes the basic contribution to the separation of 2,3-butanediol and its ester.Translated from Izvestiya Akadamii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 800–803, April, 1973.